Canonical Allele Identifier: CA2654283612

Gene: OLIG2

Linked Data

• gnomAD v4: 21-33026307-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026308del , CM000683.2:g.33026308del	GRCh38
NC_000021.8:g.34398616del , CM000683.1:g.34398616del	GRCh37
NC_000021.7:g.33320486del	NCBI36
NG_011834.1:g.5378del

Transcript Alleles

HGVS	Amino-acid change
ENST00000382357.4:c.-63+282del MANE Select	ENSP00000371794.3:n.-63+282del
ENST00000333337.3:c.-555del	ENSP00000331040.3:n.-555del
ENST00000382357.3:c.-63+282del	ENSP00000371794.3:n.-63+282del
ENST00000430860.1:c.-63+48del	ENSP00000391183.1:n.-63+48del
NM_005806.3:c.-63+282del	NP_005797.1:n.-63+282del
XM_005260908.1:c.-63+48del	XP_005260965.1:n.-63+48del
NM_005806.4:c.-63+282del MANE Select	NP_005797.1:n.-63+282del